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FDA 510(k)

MODEL VPW2877F8, MAMMO 5 POWER SUPPLY

K-Number: K942778 · 1994-07-29

ApplicantVarian Assoc., Inc.
Decision Date1994-07-29
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL VPW2877F8, MAMMO 5 POWER SUPPLY is the device name listed in this FDA 510(k) record. The listed applicant is Varian Assoc., Inc.. It received FDA 510(k) clearance on 1994-07-29 under 510(k) number K942778. The device is classified under product code IZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL VPW2877F8, MAMMO 5 POWER SUPPLY?

MODEL VPW2877F8, MAMMO 5 POWER SUPPLY is a medical device that received FDA 510(k) clearance on 1994-07-29. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K942778.

When did MODEL VPW2877F8, MAMMO 5 POWER SUPPLY receive FDA 510(k) clearance?

MODEL VPW2877F8, MAMMO 5 POWER SUPPLY received FDA 510(k) clearance on 1994-07-29, under 510(k) number K942778.

Who is the listed applicant for MODEL VPW2877F8, MAMMO 5 POWER SUPPLY?

The FDA 510(k) record lists Varian Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL VPW2877F8, MAMMO 5 POWER SUPPLY?

The FDA product code for MODEL VPW2877F8, MAMMO 5 POWER SUPPLY is IZO.

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Other records listing Varian Assoc., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K000922PROTON VISIONK992762BRACHYVISION 6.0K992751SOMAVISIONK992753CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEMK990085MILLENNIUM MLC -120K980601VARISOURCE WRIGHT VAGINAL CUFF APPLICATOR FOR VARIAN VARISOURCE REMOTE HIGH DOSE RATE AFTERIOADER

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Related Devices (Code: IZO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K954666MPH50, MPH65, AND MPH80GE Medical SystemsK953582HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATORVarian Canada, Inc.K953831N 800 HFNucletron-Oldelft Corp.K952822SHIMADZU X-RAY HIGH VILTAGE GENERATOR AHD150GShimadzu Corp.K952265MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATORControl-X, Inc.K950883POLYDOROS SX 65 AND 80Siemens Medical Solutions USA, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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